Uv-A 1978
DOI: 10.1007/978-1-4684-2475-1_5
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Effects of Ultraviolet Radiation on Microorganisms and Animal Cells

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Cited by 5 publications
(5 citation statements)
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“…When all the photon energy is transferred to the atoms and molecules that absorb it, the resulting excited states may lead to protein alteration and enzyme inactivation, which may hamper key biologic systems, e.g. through the splitting of peptide bonds, the alteration of sulfide and disulfide bonds, and photochemical oxidation [ 33 , 34 ]. Cyclobutane pyrimidine dimers, which are formed between two adjacent pyrimidines in the same strand of DNA by the cross-linking of cytosine and thymine, are considered the most important products of UV-induced damage to the DNA; they cause local denaturation of the DNA helix, prevent DNA repair, inhibit DNA replication and protein synthesis, damage RNA, lead to the loss of essential metabolic activities and cause cellular death [ 7 , 8 ].…”
Section: Discussionmentioning
confidence: 99%
“…When all the photon energy is transferred to the atoms and molecules that absorb it, the resulting excited states may lead to protein alteration and enzyme inactivation, which may hamper key biologic systems, e.g. through the splitting of peptide bonds, the alteration of sulfide and disulfide bonds, and photochemical oxidation [ 33 , 34 ]. Cyclobutane pyrimidine dimers, which are formed between two adjacent pyrimidines in the same strand of DNA by the cross-linking of cytosine and thymine, are considered the most important products of UV-induced damage to the DNA; they cause local denaturation of the DNA helix, prevent DNA repair, inhibit DNA replication and protein synthesis, damage RNA, lead to the loss of essential metabolic activities and cause cellular death [ 7 , 8 ].…”
Section: Discussionmentioning
confidence: 99%
“…When all photon energy is transferred to absorbing atoms and molecules, the resulting excited state may lead to proteins alterations and enzyme inactivation hampering key biologic systems, e.g. through the split of peptide, alteration of sul de and disul de bonds and photochemical oxidations [30,31]. In the DNA, pyrimidine dimers and cross-linking between cytosine and thymine are considered the most important UV photoproducts formed between two adjacent pyrimidines in the same strand of DNA, resulting in the production of cyclobutane pyrimidine dimers which cause local denaturation of the DNA helix, prevention of DNA repair, inhibition of DNA replication and protein synthesis, RNA damage, loss of essential metabolic activities, and cellular death [7,8].…”
Section: Discussionmentioning
confidence: 99%
“…That UV-A has different photobiological effects than UV-B may be significant in systemic photosensitivity (Table I) DNA repair synthesis, UV-A had either no effect or increased DNA repair synthesis [57]. Although UV-B may be more efficient in causing damage to DNA through direct absorption, UV-A has little effect on DNA without sensitization or activation of a secondary molecule ('chromophore') which forms a DNA cross-linking agent that may inhibit lymphocyte proliferation [7]. In skin as well as in lymphocytes, chromophore action is partly mediated by activated oxygen species which may contribute to damage of cell membranes or DNA [7,58,59].…”
Section: Pathogenesis Of Photosensitivitymentioning
confidence: 99%
“…Although UV-B may be more efficient in causing damage to DNA through direct absorption, UV-A has little effect on DNA without sensitization or activation of a secondary molecule ('chromophore') which forms a DNA cross-linking agent that may inhibit lymphocyte proliferation [7]. In skin as well as in lymphocytes, chromophore action is partly mediated by activated oxygen species which may contribute to damage of cell membranes or DNA [7,58,59]. Splenocytes from SLE murine models appear to be more sensitive to UV-A-induced oxidative stress than normal splenocytes [8,9].…”
Section: Pathogenesis Of Photosensitivitymentioning
confidence: 99%
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